Study Summary
This trial is designed to see if mindfulness meditation intervention classes improve psychosocial health outcomes, as well as examining changes in the brain that might occur following the mindfulness meditation intervention.
Eligible Conditions
- Psychosocial Functioning
- Inflammation
- Depression and Anxiety
Treatment Effectiveness
Effectiveness Progress
Study Objectives
4 Primary · 11 Secondary · Reporting Duration: Baseline and at 8 weeks
Week 8
Anhedonia
Anxiety
Compassion for others
Depression
Inflammation
Loneliness
Mindfulness
Perceived stress
Positive and negative affect
Psychological well-being
Rumination
Savoring strategies
Self-compassion
Self-concept
Sleep disruption (sleep latency, sleep duration, sleep efficiency, sleep disturbance and daytime dysfunction)
Trial Safety
Safety Progress
Trial Design
2 Treatment Groups
Wait list control
1 of 2
Mindfulness meditation intervention
1 of 2
Active Control
Experimental Treatment
60 Total Participants · 2 Treatment Groups
Primary Treatment: Mindfulness Meditation classes · No Placebo Group · N/A
Mindfulness meditation intervention
Behavioral
Experimental Group · 1 Intervention: Mindfulness Meditation classes · Intervention Types: BehavioralWait list controlNoIntervention Group · 1 Intervention: Wait list control · Intervention Types:
Trial Logistics
Trial Timeline
Screening: ~3 weeks
Treatment: Varies
Reporting: baseline and at 8 weeks
Who is running the clinical trial?
University of California, Los AngelesLead Sponsor
1,414 Previous Clinical Trials
6,763,057 Total Patients Enrolled
1 Trials studying Psychosocial Functioning
240 Patients Enrolled for Psychosocial Functioning
Julienne E Bower, Ph.D.Principal InvestigatorUniversity of California, Los Angeles
2 Previous Clinical Trials
312 Total Patients Enrolled
1 Trials studying Psychosocial Functioning
240 Patients Enrolled for Psychosocial Functioning
Eligibility Criteria
Age Any Age · All Participants · 3 Total Inclusion Criteria
Mark “Yes” if the following statements are true for you:You are a student at UCLA.\n
Who else is applying?
What state do they live in?
| California | 100.0% |
How old are they?
| 18 - 65 | 100.0% |
What site did they apply to?
| University of California, Los Angeles | 100.0% |
What portion of applicants met pre-screening criteria?
| Met criteria | 60.0% |
| Did not meet criteria | 40.0% |
How responsive is this trial?
Most responsive sites:
- University of California, Los Angeles: < 24 hours
Typically responds via
| 100.0% | |
Average response time
- < 1 Day
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Conditions
Cancer Related
Treatments